Oncotarget

Research Papers:

HOXB13 and ALX4 induce SLUG expression for the promotion of EMT and cell invasion in ovarian cancer cells

Hong Yuan _, Hiroaki Kajiyama, Satoko Ito, Dan Chen, Kiyosumi Shibata, Michinari Hamaguchi, Fumitaka Kikkawa and Takeshi Senga

PDF  |  HTML  |  Supplementary Files  |  How to cite  |  Order a Reprint

Oncotarget. 2015; 6:13359-13370. https://doi.org/10.18632/oncotarget.3673

Metrics: PDF 1200 views  |   HTML 1285 views  |   ?  


Abstract

Hong Yuan1, Hiroaki Kajiyama1, Satoko Ito2, Dan Chen2, Kiyosumi Shibata1, Michinari Hamaguchi2, Fumitaka Kikkawa1, Takeshi Senga2

1Department of Obstetrics and Gynecology, Nagoya University Graduate School of Medicine, Nagoya, 466-8550, Japan

2Division of Cancer Biology, Nagoya University Graduate School of Medicine, Nagoya, 466-8550, Japan

Correspondence to:

Hiroaki Kajiyama, e-mail: kajiyama@med.nagoya-u.ac.jp

Takeshi Senga, e-mail: tsenga@med.nagoya-u.ac.jp

Keywords: EMT, HOXB13, ALX4, ovarian cancer, invasion

Received: January 26, 2015     Accepted: March 25, 2015     Published: April 10, 2015

ABSTRACT

Homeoproteins, a family of transcription factors that have conserved homeobox domains, play critical roles in embryonic development in a wide range of species. Accumulating studies have revealed that homeoproteins are aberrantly expressed in multiple tumors and function as either tumor promoters or suppressors. In this study, we show that two homeoproteins, HOXB13 and ALX4, are associated with epithelial to mesenchymal transition (EMT) and invasion of ovarian cancer cells. HOXB13 and ALX4 formed a complex in cells, and exogenous expression of either protein promoted EMT and invasion. Conversely, depletion of either protein suppressed invasion and induced reversion of EMT. SLUG is a C2H2-type zinc-finger transcription factor that promotes EMT in various cell lines. Knockdown of HOXB13 or ALX4 suppressed SLUG expression, and exogenous expression of either protein promoted SLUG expression. Finally, we showed that SLUG expression was essential for the HOXB13- or ALX4-mediated EMT and invasion. Our results show that HOXB13/SLUG and ALX4/SLUG axes are novel pathways that promote EMT and invasion of ovarian cancer cells.


Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 3673